Хайлтын үр дүнгүүд - Kevin Colclough

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  1. 1
    Mutations in the genes encoding the transcription factors hepatocyte nuclear factor 1 alpha (<i>HNF1A</i>) and 4 alpha (<i>HNF4A</i>) in maturity-onset diabetes of the young

    Mutations in the genes encoding the transcription factors hepatocyte nuclear factor 1 alpha (<i>HNF1A</i>) and 4 alpha (<i>HNF4A</i>) in maturity-onset diabetes of the young -н Sian Ellard, Kevin Colclough

    Хэвлэсэн 2006
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    Artigo
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  2. 2
    Syndromic Monogenic Diabetes Genes Should Be Tested in Patients With a Clinical Suspicion of Maturity-Onset Diabetes of the Young

    Syndromic Monogenic Diabetes Genes Should Be Tested in Patients With a Clinical Suspicion of Maturity-Onset Diabetes of the Young -н Kevin Colclough, Sian Ellard, Andrew T. Hattersley, Kashyap Patel

    Хэвлэсэн 2021
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    Artigo
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  3. 3
    Monogenic diabetes: a gateway to precision medicine in diabetes

    Monogenic diabetes: a gateway to precision medicine in diabetes -н Haichen Zhang, Kevin Colclough, Anna L. Gloyn, Toni I. Pollin

    Хэвлэсэн 2021
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    Revisão
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  4. 4
    Maturity-onset diabetes of the young (MODY): how many cases are we missing?

    Maturity-onset diabetes of the young (MODY): how many cases are we missing? -н Beverley M. Shields, Sarah Hicks, Maggie Shepherd, Kevin Colclough, Andrew T. Hattersley, Sian Ellard

    Хэвлэсэн 2010
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    Artigo
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  5. 5
    Mutations in the Genes Encoding the Transcription Factors Hepatocyte Nuclear Factor 1 Alpha and 4 Alpha in Maturity-Onset Diabetes of the Young and Hyperinsulinemic Hypoglycemia

    Mutations in the Genes Encoding the Transcription Factors Hepatocyte Nuclear Factor 1 Alpha and 4 Alpha in Maturity-Onset Diabetes of the Young and Hyperinsulinemic Hypoglycemia -н Kevin Colclough, Christine Bellanné‐Chantelot, Cécile Saint‐Martin, Sarah E. Flanagan, Sian Ellard

    Хэвлэсэн 2013
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    Artigo
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  6. 6
    Prevalence of Vascular Complications Among Patients With Glucokinase Mutations and Prolonged, Mild Hyperglycemia

    Prevalence of Vascular Complications Among Patients With Glucokinase Mutations and Prolonged, Mild Hyperglycemia -н Anna Steele, Beverley M. Shields, Kirsty J. Wensley, Kevin Colclough, Sian Ellard, Andrew T. Hattersley

    Хэвлэсэн 2014
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    Artigo
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  7. 7
    Cross-sectional and longitudinal studies suggest pharmacological treatment used in patients with glucokinase mutations does not alter glycaemia

    Cross-sectional and longitudinal studies suggest pharmacological treatment used in patients with glucokinase mutations does not alter glycaemia -н Amanda Stride, Beverley M. Shields, Olivia Gill-Carey, Ali Chakera, Kevin Colclough, Sian Ellard, Andrew T. Hattersley

    Хэвлэсэн 2013
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    Artigo
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  8. 8
    South Asian individuals with diabetes who are referred for MODY testing in the UK have a lower mutation pick-up rate than white European people

    South Asian individuals with diabetes who are referred for MODY testing in the UK have a lower mutation pick-up rate than white European people -н Shivani Misra, Beverley M. Shields, Kevin Colclough, Desmond G. Johnston, Nick Oliver, Sian Ellard, Andrew T. Hattersley

    Хэвлэсэн 2016
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    Carta
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  9. 9
    Update on mutations in glucokinase (<i>GCK</i>), which cause maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemic hypoglycemia

    Update on mutations in glucokinase (<i>GCK</i>), which cause maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemic hypoglycemia -н Kara Osbak, Kevin Colclough, Cécile Saint‐Martin, Nicola L. Beer, Christine Bellanné‐Chantelot, Sian Ellard, Anna L. Gloyn

    Хэвлэсэн 2009
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    Revisão
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  10. 10
    Use of HbA1c in the Identification of Patients with Hyperglycaemia Caused by a Glucokinase Mutation: Observational Case Control Studies

    Use of HbA1c in the Identification of Patients with Hyperglycaemia Caused by a Glucokinase Mutation: Observational Case Control Studies -н Anna Steele, Kirsty J. Wensley, Sian Ellard, Rinki Murphy, Maggie Shepherd, Kevin Colclough, Andrew T. Hattersley, Beverley M. Shields

    Хэвлэсэн 2013
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    Artigo
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  11. 11
    Persistent Hyperinsulinemic Hypoglycemia and Maturity-Onset Diabetes of the Young Due to Heterozygous <i>HNF4A</i> Mutations

    Persistent Hyperinsulinemic Hypoglycemia and Maturity-Onset Diabetes of the Young Due to Heterozygous <i>HNF4A</i> Mutations -н Ritika R. Kapoor, Jonathan M. Locke, Kevin Colclough, J K Wales, Jennifer Conn, Andrew T. Hattersley, Sian Ellard, Khalid Hussain

    Хэвлэсэн 2008
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    Artigo
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  12. 12
    Improvements in Awareness and Testing Have Led to a Threefold Increase Over 10 Years in the Identification of Monogenic Diabetes in the U.K.

    Improvements in Awareness and Testing Have Led to a Threefold Increase Over 10 Years in the Identification of Monogenic Diabetes in the U.K. -н Lewis Pang, Kevin Colclough, Maggie Shepherd, Joanne McLean, Ewan R. Pearson, Sian Ellard, Andrew T. Hattersley, Beverley M. Shields

    Хэвлэсэн 2022
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    Artigo
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  13. 13
    Type 1 Diabetes Genetic Risk Score: A Novel Tool to Discriminate Monogenic and Type 1 Diabetes

    Type 1 Diabetes Genetic Risk Score: A Novel Tool to Discriminate Monogenic and Type 1 Diabetes -н Kashyap Patel, Richard A. Oram, Sarah E. Flanagan, Elisa De Franco, Kevin Colclough, Maggie Shepherd, Sian Ellard, Michael N. Weedon, Andrew T. Hattersley

    Хэвлэсэн 2016
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    Artigo
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  14. 14
    HNF1B Mutations Are Associated With a Gitelman-like Tubulopathy That Develops During Childhood

    HNF1B Mutations Are Associated With a Gitelman-like Tubulopathy That Develops During Childhood -н Shazia Adalat, Wesley Hayes, William Bryant, John Booth, Adrian S. Woolf, Robert Kleta, Sandra Subtil, Rhian Clissold, Kevin Colclough, Sian Ellard, Detlef Böckenhauer

    Хэвлэсэн 2019
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    Artigo
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  15. 15
    Evaluation of Evidence for Pathogenicity Demonstrates That <i>BLK</i>, <i>KLF11</i>, and <i>PAX4</i> Should Not Be Included in Diagnostic Testing for MODY

    Evaluation of Evidence for Pathogenicity Demonstrates That <i>BLK</i>, <i>KLF11</i>, and <i>PAX4</i> Should Not Be Included in Diagnostic Testing for MODY -н Thomas W. Laver, Matthew N. Wakeling, Olivia Knox, Kevin Colclough, Caroline F. Wright, Sian Ellard, Andrew T. Hattersley, Michael N. Weedon, Kashyap Patel

    Хэвлэсэн 2022
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    Artigo
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  16. 16
    A heterozygous activating mutation in the sulphonylurea receptor SUR1 (ABCC8) causes neonatal diabetes

    A heterozygous activating mutation in the sulphonylurea receptor SUR1 (ABCC8) causes neonatal diabetes -н Peter Proks, Amanda L. Arnold, Jan Bruining, Christophe A. Girard, Sarah E. Flanagan, Brian Larkin, Kevin Colclough, Andrew T. Hattersley, Frances M. Ashcroft, Sian Ellard

    Хэвлэсэн 2006
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    Artigo
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  17. 17
    Exome sequencing reveals a de novo POLD1 mutation causing phenotypic variability in mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome (MDPL)

    Exome sequencing reveals a de novo POLD1 mutation causing phenotypic variability in mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome (MDPL) -н Sahar Elouej, Ana Beleza‐Meireles, Richard Caswell, Kevin Colclough, Sian Ellard, Jean-Pierre Desvignes, Christophe Béroud, Nicolas Lévy, Shehla Mohammed, Annachiara De Sandre‐Giovannoli

    Хэвлэсэн 2017
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    Artigo
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  18. 18
    Common Genetic Variants Modify Disease Risk and Clinical Presentation in Monogenic Diabetes

    Common Genetic Variants Modify Disease Risk and Clinical Presentation in Monogenic Diabetes -н James H. Leech, Robin N. Beaumont, Ankit M Arni, V. Kartik Chundru, Luke N Sharp, Kevin Colclough, Andrew T. Hattersley, Michael N. Weedon, Kashyap Patel

    Хэвлэсэн 2025
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    Pré-impressão
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  19. 19
    Characteristics of maturity onset diabetes of the young in a large diabetes center

    Characteristics of maturity onset diabetes of the young in a large diabetes center -н Christina Chambers, Alexandra Fouts, Fran Dong, Kevin Colclough, Zhenyuan Wang, Sat Dev Batish, Malgorzata Jaremko, Sian Ellard, Andrew T. Hattersley, Georgeanna J. Klingensmith, Andrea K. Steck

    Хэвлэсэн 2015
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    Artigo
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  20. 20
    Improved genetic testing for monogenic diabetes using targeted next-generation sequencing

    Improved genetic testing for monogenic diabetes using targeted next-generation sequencing -н Sian Ellard, Hana Lango Allen, Elisa De Franco, Sarah E. Flanagan, Gerald Hysenaj, Kevin Colclough, Jayne Houghton, Maggie Shepherd, Andrew T. Hattersley, Michael N. Weedon, Richard Caswell

    Хэвлэсэн 2013
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    Artigo
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